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Volumn 46, Issue 5, 2000, Pages 585-587
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The molecular and genetic base of congenital transport defects
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Author keywords
[No Author keywords available]
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Indexed keywords
CHLORIDE ION;
GLUCOSE TRANSPORTER;
HEXOSE;
MAGNESIUM;
SODIUM CHLORIDE;
SODIUM ION;
TRANSMEMBRANE CONDUCTANCE REGULATOR;
AMINOACIDURIA;
CYSTIC FIBROSIS;
CYSTINURIA;
DIARRHEA;
GASTROINTESTINAL DISEASE;
GENE MUTATION;
GENETIC DISORDER;
GENOTYPE;
HUMAN;
ION TRANSPORT;
MALABSORPTION;
MENKES SYNDROME;
NON INSULIN DEPENDENT DIABETES MELLITUS;
PHENOTYPE;
PRIORITY JOURNAL;
REVIEW;
WILSON DISEASE;
BIOLOGICAL TRANSPORT;
GENOTYPE;
HUMANS;
MALABSORPTION SYNDROMES;
MOLECULAR BIOLOGY;
MUTATION;
PHENOTYPE;
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EID: 0034099516
PISSN: 00175749
EISSN: None
Source Type: Journal
DOI: 10.1136/gut.46.5.585 Document Type: Review |
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Times cited : (7)
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References (27)
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